FDA Inspection 874728 — Keurig Dr Pepper Inc.

Keurig Dr Pepper Inc. — FEI 3024786768

The FDA completed an inspection of Keurig Dr Pepper Inc. on Apr 11, 2014 in Frisco, TX. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Food/Cosmetics.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Apr 11, 2014
Fiscal Year
2014
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Frisco, TX (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.